Canonical Allele Identifier: CA2002674487
Community Standard Title: NC_000011.10:g.116655150C=
Gene: LINC02702 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116655150C= , CM000673.2:g.116655150C= GRCh38
NC_000011.9:g.116525867C= , CM000673.1:g.116525867C= GRCh37
NC_000011.8:g.116031077C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_135069.1:n.272+2097C=
XR_246484.2:n.272+2097C=
XR_948058.1:n.371C=